M 944 (Divalproex Sodium Delayed-Release 250 mg)

This pill with imprint "M 944" is Blue, Round and has been identified as Divalproex sodium delayed-release 250 mg. It is manufactured by Mylan Pharmaceuticals Inc..

Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; epilepsy; borderline personality disorder (and more), and belongs to the drug class fatty acid derivative anticonvulsants. When treating epilepsy and manic episodes associated with bipolar disorder: There is positive evidence of human fetal risk during pregnancy. When treating migraine: Not for use in pregnancy. Divalproex sodium 250 mg is not a controlled substance under the Controlled Substance Act (CSA).

Divalproex sodium delayed-release

Imprint:

M 944

Strength:

250 mg

Color:

Blue

Size:

11.00 mm

Shape:

Round

Availability:

Prescription only

Drug Class:

Fatty acid derivative anticonvulsants

Pregnancy Category:

D - Positive evidence of risk - When treating epilepsy and manic episodes associated with bipolar disorder
X - Not for use in pregnancy - When treating migraine

CSA Schedule:

Not a controlled drug

Manufacturer:

Mylan Pharmaceuticals Inc.

National Drug Code (NDC):

00378-1044

Inactive Ingredients:

ferrosoferric oxide
silicon dioxide
copovidone
croscarmellose sodium
FD&C Blue No. 2
FD&C Yellow No. 6
hypromelloses
lactose monohydrate
methacrylic acid - ethyl acrylate copolymer (1:1) type a
microcrystalline cellulose
polydextrose
polyethylene glycol
polysorbate 80
polyvinyl alcohol
propylene glycol
sodium hydroxide
magnesium silicate
titanium dioxide
triacetin
triethyl citrate

Note: Inactive ingredients may vary.

Imprint Code FAQ's

Other Manufacturers / Repackagers:

NDC Code	Manufacturer / Repackager
51079-0474	UDL Laboratories Inc

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